@LLS - See what's happening
1 2 3 4 Previous Next

@LLS

53 Posts

baldacious_logo.jpg

With Valentine's Day right around the corner, there's no better way to show your love for cancer patients than by going Totally Baldacious. Register today and commit to shaving your head or coloring your hair to raise funds for life-saving cancer research. Go Totally Baldacious and help cure cancers!

 

Use the Be Baldacious widget or Facebook Application to tell your social networking friends and boldly show your solidarity with cancer patients and their families.

 

We don't think there's a more audacious way to show you care.

 

Begin by signing up on www.totallybaldacious.org and start fundraising today! And if you're already fundraising for The Leukemia & Lymphoma Society (through Team In Training, the Light The Night Walk or the Man & Woman of the Year campaigns), contact your campaign directors for tips on how to apply this concept to your fundraising goals.

 

Follow the @LLS Blog for daily posts on this campaign throughout February -- and send your stories and pics to baldacious@lls.org  with pride.

 

Happy Valentine's Day and thank you for spreading the love!

0 Comments Permalink

baldacious_logo.jpg

Do you know someone with cancer? Have you wondered how you can show your support? This Valentine’s Day, we're launching an exciting new fundraising campaign - Totally Baldacious. When you shave or color your hair, you are showing your solidarity with cancer patients, raise awareness about cancer, and help raise money for The Leukemia & Lymphoma Society.

Amy Barlett is the Totally Baldacious Honored Hero.  Amy holds a special place in our heart as a non-Hodgkin lymphoma survivor who’s also a multi-event Team In Training alumna!  When Amy lost her hair during treatment, she found the silver lining...noting that,  “When you’re bald you don’t have to worry about a bad hair day.”

 

Read this Q&A with Amy:

https://reg.dojiggy.com/images/uploads/6885/AmyForWeb.jpg

LLS:  In May you celebrate 3 years in remission. Congratulations! When you began treatment and lost your hair did anyone shave their head to show their solidarity with you?

Amy: Twenty of my male friends all let me shave their heads before my sister shaved mine in front of about 100 of my family and friends.  I shaved mullets, mohawks, tails...you name it.

 

LLS: How did you feel when you realized that they were doing that?

Amy: The day I found out I was going to lose my hair I decided I wanted to throw a party and lose it on my own terms.  Over 100 people showed up to the party.  I was amazed and honored.  When the boys lined up, it was so unexpected yet made the evening more fun.  For us, it was about turning a sad part of cancer in to a happy memory.  When I think of losing my hair, I go back and look at the pictures of the party.  It was seriously one of the best nights of my whole life.

 

LLS: Part of the reason we've launched Totally Baldacious just before Valentine's Day is to spread love to our patients and raise awareness for the importance of showing support for patients. When you were undergoing treatment, how important was your support system to you?

Amy: Having a support system is extremely important.  I am fiercely independent and had a hard time accepting help at first.  Asking for help actually makes you stronger.  It is not a sign of weakness.  Knowing my friends shaved their heads to be "on my team" meant everything to me.

 

LLS: What LLS resources did you take advantage of at the time?

Amy: The night of my party we also accepted donations and had a silent auction with all money raised going to LLS.  We raised over $20,000 that evening.  I joined Team In Training during my treatment to give me a good fitness goal for the end of the chemo and radiation road.  It motivated me to go for walks and stay active even in the darkest days.  Saturdays I knew I would see the team and we inspired each other.  I was so grateful to the other participants for raising money for people like me - with cancer.  And they thanked me for providing them motivation to get up, log the miles, and raise the money.

 

LLS: You have a blog, www.ichoosehope.com and a twitter profile (@amyebartlett)  - how will you be promoting Totally Baldacious online through February?

Amy: While I won't be shaving my head again for the Totally Baldacious month, I would love to connect with patients and hear other inspiring stories of the best parts of being bald.  Like - how fun accessorizing your head can be...big sunglasses, scarves, hoop earrings.  Just decorate it!  Tattoos are super fun, or henna art could also be beautiful.  I wish I would have thought of the artistic things when I was bald.  Turn it in to an opportunity to be creative and put a smile on your face.  And remember, you can't have a bad hair day if you are bald.  That is a bonus.

 

LLS:  Will you be using the Be Baldacious widget to bald yourself and tell your friends?

Amy: Yes, I will share this with my friends and family.

 

LLS:  Amy, one of the most remarkable things about you and your story is your connection to Team In Training. How many times have you participated in Team In Training?

Amy: I had been a participant in TNT four times before I was every diagnosed.  In a strange way, I believe my early involvement could have played a role in my successful treatment.  Perhaps some of the money I raised over the years helped advance research that has given me a second chance at life...  I have participated two times after being a patient, and I am signing up this year, again, for the Nike Women's Marathon in San Francisco.

 

LLS: And how much have you raised to date to fight cancer?

Amy: Somewhere in the $60,000 range which truly boggles my mind.  The dark times in our lives can truly reveal the best qualities in people.  I receive donations when I am not even officially training.  People write a check and say "this is for your next one" which is so amazing.

 

LLS:  I understand you are considering participating again, is that true?

Amy: Yes, I sure am..  I want to eventually do an Olympic distance triathlon, but I haven't worked up the courage for that yet.  For now I am sticking with 1/2 and full marathons.

 

LLS:   What would you say to others who are contemplating Team In Training but have never trained before?

Amy:  It will be one of the best experiences of your life.

 

LLS:  What's the best thing about your Team In Training experience?

Amy:  Knowing that I am making a difference in someone's life.  My dream one day is for us to be able to say "Remember when people used to get cancer?"

 

Learn more about:

baldacious_logo.jpg                    tnt.jpg

0 Comments Permalink

We approached Team In Training alumni and President of Karhu North America, Jay Duke, to feature his story on this blog.  Jay's passion for our mission is an inspiration, just as Karhu's product partnership is a welcome alliance. Here's Jay's story:

 

llsstory2.jpg


One of my wife's best friends - her sister and Godmother to our firstborn - was diagnosed with Leukemia in September 2001. A devoted oncology nurse and impassioned advocate for her patients, Mary June knew the climb and was a natural fighter. She waged a fierce battle and one year later, as we all expected, the doctors diagnosed her as cancer-free. The entire family celebrated the victory of her one-year remission with a festive dinner party.


The celebration was short lived as the cancer reappeared 18 months later. Knowing full well the difficulty of the second time around, she did not waver in her fight for life. My last moments with Mary June were at my daughter's birthday party just days before she passed away the third of September 2005. Even in her weakened state, Mary June was there with us and for us - her family. Mary June asked us never to forget her, an impossible thought to those who knew her, including those in oncology community who unimaginably lost one of their own to the very illness.


In Mary June's memory I joined my first LLS fundraising event, a sprint triathlon, in 2006. I have participated in a minimum of one LLS event every year since, including this past 2009 Boston Marathon. Last year I joined the venture to build KARHU and CRAFT and fortunately can now elevate a personal passion with a corporate partnership to support the mission of LLS and a cause I am committed to for life. I can only hope this partnership will be one way to spare others from similar heartache.


Thank you, Jay, for allowing us to post your story and for all you do to help fund life-saving cancer research!

 

 

You can help LLS fund life-saving research by clicking here to begin shopping. 20% of your total order will directly benefit LLS.

0 Comments Permalink

Today, February 1, more than 100 blood cancer volunteers from The Leukemia & Lymphoma Society’s six New York chapters will join key legislative leaders in Albany on health care to urge support for legislation to increase access to life-saving health care services for cancer patients.  But just because you were not able to make the trip to the Capitol building doesn’t mean you can’t still join in the excitement of New York’s State Mission Day!


There are two ways that you can still participate in the day:


1. ) Please visit LLS’s Legislative Action Center and send a pre-drafted email to your representatives urging them to support our legislative agenda, and
2. ) you can follow the day online. We will be posting updates, volunteer feedback, photos and video right here on the LLS Blog and several other online outlets, including Facebook, Twitter and Flickr.


So check in from time-to-time and be a part of New York’s 2010 State Mission Day!

 

0 Comments Permalink

The following blog was originally posted on the Offshore Sailing School Blog (see: www.offshoresailingschool.com/blog) by Offshore Sailing School CEO and President, Doris Colgate. It's featured here with her permission:

 

As most of you know, Offshore Sailing School is a national sponsor of The Leukemia Cup Regattas – a fund-raising arm of the Leukemia & Lymphoma Society (LLS). Yesterday I received a “Thank You” email I want to share with all of you. The author gave me permission and I have kept out names and locations to protect her from spammers, but the story is true, and heartbreaking. Before I received this we had already decided to donate $25 of every regular course tuition we teach in 2010 to LLS. If you are considering sailing lessons, learning to sail, or a bareboat cruising course, this might push you over the edge. I know there is a lot of tragedy surrounding all of us these days, particularly as we see what is happening in Haiti. But many diseases are now cured because of the incredible resesarch done to find cures for blood cancers.

 

Here is her story:

“On Halloween at 4:30 p.m., my fiancee was diagnosed with Leukemia AML-M3. He was 40 years old, days away from his 41st birthday. He had never had any symptoms of anything more than a fever for a few days and a little difficulty breathing, which is what brought us to an ER unit three times, the last on October 30th. He was diagnosed with walking pneumonia and pneumonia and was transferred to a hospital that Friday night, where he was diagnosed with AML with the devastating words that if we did not start chemo that night he would not be alive in a week. Unfortunately, those words would ring true even though we did start chemo less than six hours after his diagnosis.


“Thirty-six hours is never enough time to prepare to lose your best friend, your future, your lover, your life and then to watch him slip away so quickly. It is a disease that I am only now beginning to wrap my brain around how it attacks the body.  My fiancee was an unforgettable man. He got his first sailboat at age 12. He spent every summer on his boat and eventually settled in a sailing community. There were several years that he lived aboard. I can remember the smile on his face like it was yesterday when we watched 12 Metres sailing last fall.


“He was an amazing man, with a mechanical engineering degree, but his hobbies made him who he was  – an accomplished sailor who loved the sea. He held a Merchant Marines Sea Captains License and a private pilots license. At his funeral all of his pall bearers wore captain’s hats in his honor. At any given time he was the entertainer of entertainers – the one that everyone ALWAYS wanted to be around.


“I want to say thank you for all that you do and have done for the Leukemia & Lymphoma Society. You cannot imagine how comforting it is to know that people out there care and offer time and effort to a cause so close to my heart. The day we sat in the hospital the first time I did not even know how to spell Leukemia and now I feel like I am becoming an expert on it.


“I am just starting to get back to life after all that happened. I have joined LLS and would really love to come participate at some point in one of your weekends. I want to give back and be involved in anything that I can to help other people that might be in our shoes one day. I cannot do anything to help or save my fiancee but I can try to help other people the way you are.”

 

I cried when I read her email. I hope to meet her someday soon and give her a strong hug for her candor and resolve. You may not know how many sailors have been afflicted by lymphoma, leukemia or myeloma -and how many sailors have someone close to them or in their circle of friends who are going through treatment or are in remission. We always said the world was small, and it becomes smaller and smaller as our circle of sailing friends gather around this very important cause. I hope you will too.

 

 

DC10.jpg

Doris Colgate, Chief Executive Officer and President,

Offshore Sailing School

0 Comments Permalink

If you or someone you care about is a young adult who is dealing with Hodgkin lymphoma, you’ll want to listen to Monday’s Stupid Cancer Show, called “Who The Hell Is Hodgkin’s?”. This show will feature guests Ethan Zohn, winner of Survivor: Africa who is now undergoing treatment for Hodgkin lymphoma, and our own Hildy Dillon, Senior Vice President, Patient Services.

Show Name: Who The Hell Is Hodgkin’s?
Date: 12/28/2009
Time: 9:00 PM ET
Length: 1 hr 30 min
Call-in Number: 347.215.6845

For more information and to set a reminder, visit this show’s page on Blog Talk Radio.

This web-based program is produced by the Stupid Cancer Show of I’m Too Young For This! Cancer Foundation (i[2]y).

Not able to join the call? Call us with your Hodgkin lymphoma or other blood cancer questions at 1.800.955.4572.

0 Comments Permalink

For three days this weekend, from Friday, December 11th through Sunday, December 13th, Club Monaco will be offering 25% off all of their merchandise to shoppers who bring in this flyer when shopping in their stores.

 

dance.gif


Club Monaco shoppers will receive 25% off, with 10% of the proceeds benefitting The Leukemia & Lymphoma Society (LLS).


Download the flyer today, share it with friends, and be sure to stop by Club Monaco this weekend to conduct your holiday shopping "in style"! When you do, you'll be helping blood cancer patients everywhere live better, longer lives.

0 Comments Permalink

LTN_C lo res jpg.jpg

 

We're fortunate that most of our National Supporting Sponsors not only share our mission, but also actively participate in our Light The Night Walks through employee teams in Light The Night Walk events throughout the country. Included among our distinguished sponsors are:

 

Bristol-Myers Squibb
A National Sponsor for 4 years, Bristol-Myers Squibb (BMS), founded in 1858, has had a long history of supporting cancer patient programs. For more about BMS and their commitment to CML, visit:  www.mycmlcare.com

 

Cephalon
Among the top ten biopharmaceutical companies in the world, Cephalon is keenly interested in improving the heath and enhancing the quality of patients lives. For more about Cephalon, visit www.cephalon.com.

 

Genentech l Biogen idec
Returning National Supporting Sponsors, Genentech l Biogen idec, also share a mission with The Leukemia & Lymphoma Society, Visit www.gene.com and www.biogenidec.comhttp://www.biogenidec.com/ for more information about these sponsors.

 

Michael C. Fina
"Celebrating each and every family's many milestones, starting with the day your loved one is cancer free" is the distinguished hope of fine jewelry and home decor designer, Michael C. Fina. Visit www.michaelcfina.com for more on this Light The Night Walk sponsor.

 

Millenium : The Takeda Oncology Company
Aspiring to be part of "the step-by-step process to cure cancer" Millenium has provided extensive support for patient education programs for blood cancer patients. Visit www.mlmn.com for more about Millennium: The Takeda Oncology Company sponsor of The Light The Night Walk.

 

Quest Diagnostics
One of the nation's largest medical testing and diagnostics companies, Quest Diagnostics has selected LLS as its national charity through 2010, in addition to serving as a National Supporting Sponsor of The Light The Night Walk. For more on our friends at Quest Diagnostics, visit www.questdiagnostics.com

 

The Leukemia & Lymphoma Society applauds our Light The Night Walk Sponsors, recognizing the impact they have had on our ability to help blood cancer patients live longer, better lives in communities across the country and in Canada.

 

Thanks to you, we're that much closer to cures!

0 Comments Permalink

Offshore Sailing School co-owner, offers sailing vacation packages from January - May to benefit LLS.

 

mini-steve_doris_portrait.jpg

Steve and Doris Colgate

 

For Doris Colgate, sailing has been a lifelong passion.  Sailing changed my life,” says Doris, who's co-owner of Offshore Sailing School. “It opened new doors, provided new and lasting friendships, treated me to the most wonderful travel opportunities, and above all - a job and partner beyond my wildest dreams!”  That “partner” is her husband, Steve Colgate, co-owner, founder and Chairman of Offshore Sailing School, one of the foremost racing sailors in the United States and the pre-eminent sailing educator worldwide.

 

The Colgates’ circle of friends in the world of sailing includes Gary Jobson, the national chair of The Leukemia Cup Regatta since 1993.  According to Doris Colgate, “we’ve known Gary since he competed in the America’s Cup in the 1970s so we were very aware of his involvement with The Leukemia Cup Regatta.  It was a total shock to us when we found out about Gary’s diagnosis of lymphoma in 1993.  Several close friends of ours’ have also been affected by blood cancers, and as the daughter of  a scientist, I’ve also been tuned into the medical community.”

 

The Colgates combined their passions to provide a special offer to sailing enthusiasts that would help raise funds and awareness for the fight against leukemia, lymphoma and myeloma. Their Offshore Sailing School is offering a special sailing training program in Florida, where participants can enjoy Captiva Island – known as “Florida’s Tahiti” - and take a sailing course, knowing $500 of their vacation package purchase will be donated to The Leukemia & Lymphoma Society.  The courses begin the weeks of January 10, 2010, January 31, 2010, April 25, 2010 and May 9, 2010.

 

Find out more about this amazing offer.

 

On behalf of Offshore Sailing School and The Leukemia & Lymphoma Society, the Colgates thank you for your support and wish both sailors and landlubbers the best for a great holiday season.

0 Comments Permalink

It may sound like a fruity idea, but it's also a lot of fun!


This year LLS is proud to be included among the featured charities in PayPal's popular year-end 'Regift the Fruitcake' campaign. By regifting a fruitcake for LLS you can help fight blood cancers and qualify for weekly prizes in the process. At the end of the campaign, which runs through December 31st, PayPal will donate to the top three Non-profits - those non-profits that raised the most through this campaign.

 

charity_banner_300x250.GIF


With your participation and promotion we hope to secure top fundraising prize - an additional $20,000 donation from PayPal.


So get in the holiday spirit and regift your Fruitcake for LLS today!


Participating is quick and easy and designed especially for Facebook and Twitter promotion. Register here and start regifting today.


Lets put those little 'fruity bars of hope' to use for a great cause!

0 Comments Permalink

At LLS we like to say that "one person can make a difference -- and YOU can be that person!" because it's true! Our volunteers throughout the U.S. and Canada are involved in every aspect of our operations and are the driving force behind much of what we're able to accomplish.

 

Emmaline Simpson and Leonard Bonneau, are two of our volunteers who are also blood cancer survivors. They recently volunteered for us at the television taping of Kaleidoscope - a celebration of Skating, Song and Survivorship, which will be aired on Thanksgiving Day, on the Fox network immediately following the football telecast.

 

kal2.jpg

Emmaline and Leonard are pictured at the live taping of Kaleidoscope at The Verizon Center in Washington, DC.


We asked both Emmaline and Leonard to share their thoughts on the show. Here's what they had to say:


Emmaline:

Kaleidoscope was an amazing event and I am so glad I was able to attend--in both a volunteer capacity and as an audience member. Meeting and talking with the folks who stopped by the LLS information table was a real honor. I was very touched by some of the stories shared by survivors who stopped by to thank LLS for their tickets. The chance to interact with these folks was one of the major reasons I signed on as a volunteer with my chapter, and I hope to get the opportunity to hear more stories as I continue volunteering.


I also thoroughly enjoyed the show, and can't thank LLS enough for my ticket. Most little girls idolize figure skaters and I was no exception, so the chance to see these skaters live was a real treat. I was touched by Dorothy Hamil's and Scott Hamilton's returns to the ice as cancer survivors, and by the transparent joy in Christi Yamaguchi and Nancy Kerrigan and so many others who skated in honor of cancer survivors. they, along with David Foster, Olivia Newton-John, and all of the other participants in the show paid a wonderful tribute to honor the folks who overcome daunting obstacles to beat the odds of a cancer diagnosis.


I'm hoping to convince my family to watch on Thanksgiving day -- I certainly wouldn't mind seeing and hearing it all over again!


Leonard:

I would just like to thank you for letting me be a part of that exciting event on behalf of The Leukemia & Lymphoma Society. I would encourage anyone who possibly can, to view the televised event on Fox! I am a big fan of all sports and I would have to rank this in the top 3 live events that I have witnessed! This event also had a couple of recording artists from past American Idol shows and cancer survivor Olivia Newton-John. The ice skating portion of the show featured Olympic Medalists such as Dorthy Hamil, Kristi Yamaguchi, Scott Hamilton, and Nancy Kerrigan.


Even though all of these performances were tremendous, the best part of the night for me was interacting with the crowd and seeing how gracious they were for the LLS being a special part of their lives. I am a survivor of CLL and being able to volunteer at this event has just brought me full circle to be able to give back in a small way, Thank You God!


If you'd like to become an LLS volunteer, like Emmaline and Leonard, fill out our Volunteer form on www.lls.org.


For more about Kaleidoscope, visit www.womenandcancer.com -- and don't miss the show, to be televised Thanksgiving Day on Fox network, immediately following the football telecast.

0 Comments Permalink

Gap_Header2.gif

 

UPDATE: Thank you to everyone who participated in this campaign! The results are in and because of you, more than $650,000 was raised for life-saving cancer resarch. Thanks for shopping!

 

 

Jennifer Donnelly is the mother of Matthew, an acute lymphocytic leukemia patient who's story is featured in the Gap Give & Get Campaign.  Gap Give & Get gives you a 30% off coupon to shop at all Gap, Inc. store, with 5% of the proceeds going to benefit The Leukemia & Lymphoma Society.

 

llsphoto.jpgJennifer shared her story with LLS:

 

How did you find out that Matthew had leukemia?


Matthew was diagnosed on December 11th, 2007, when he was two and a half years old. He hadn't been feeling well and our regular doctor thought he had a double ear infection. In fact he did have a double ear infection, but thankfully our doctor also had blood work done on Matthew, which ultimately determined that he had acute lymphocytic leukemia (ALL).  It was devastating at the time, but in hindsight we were glad he was diagnosed early on.


Before Matthew's diagnosis, had you ever heard of leukemia?


To be honest, no -- but I learned very quickly.  I also found a huge support group of people out there who are willing to help.

 

How has LLS been helpful to you and Matthew?

 

We participate in LLS's finanicial aid program and have also participated in The Light The Night Walk twice.  Matthew was also recently named the 'Boy of the Year' for the local LLS chapter here on Long Island.

 

Your son has an amazing smile.  He looks like he has a very positive outlook.

 

He does!  When he was first diagnosed, going to see the doctors so often was difficult and I would try a number of things to make it a positive experience - like dressing up in costumes. Well now, Matthew actually looks forward to going! Once when we were on vacation in Disneyland, he surprised me with "Lets go to the clinic, Mom!"   There we were, in the "happiest place on earth" and he wants to go to the clinic!

 

How is Matthew doing now?

 

Matthew's doing very well. He's in the second year of his treatment, which will continue through 2011.  We are participating in a trial.

 

A clinical trial?

 

Yes, again, before Matthew had been diagnosed, I didn't realize how important clinical trials could be to treatment options.  I found out as much as I could in advance, especially about the protocol that was suggested for Matthew.  Now, I think of all of the people who participated in trials before us and I'm grateful.  If they hadn't, I wonder where we'd be now.  Thanks to previous trials and the people who participated in them, treatments have improved.

 

Have you participated in any previous Give & Get campaign?

 

We participated in both the spring and summer campaigns.  A coupon was forwarded to me via email.  The 30% discount is terrific and knowing 5% of the sale goes back to LLS - even better!

 

Now, when I know of a business, like Gap, that gives back to LLS -- I think, "They're doing this for research, they're doing this for cures, and they're doing this for my son."  It makes me want to cry because I know the true benefit of this kind of support.


Thank you, Jennifer, for sharing your story with us and allowing us to feature Matthew in this campaign.

gap_coupon.jpg

0 Comments Permalink

Michigan Musicians and The Leukemia & Lymphoma Society Collaborate on Inspirational CD

 

LLSCoversm.gif

Legendary folk artists, Peter, Paul and Mary, and nationally acclaimed recording artists Tom Chapin, and Josh White, Jr. are a few of the many Michigan musicians featured on this CD, which was inspired by the battle several of the CD's artists have endured in the fight against cancer.

 

Now available from CDbaby.com, you may order :"As Long As I'm Here" and know that all proceeds will go to support The Leukemia & Lymphoma Society's life-saving blood cancer research.

 

Click here to place your order today!

0 Comments Permalink

Supporters of The Leukemia & Lymphoma Society are using the new LLS Toolbar, raising  money for the cause with every Internet search and online purchase

 

goodsearch.gif

 

What if even a fraction of the $140 billion generated by search engine advertising and online shopping was directed towards finding a cure for blood cancers and improving the quality of life of patients and their families?

 

The Leukemia & Lymphoma Society recently teamed up with GoodSearch.com to launch the new Leukemia & Lymphoma Society Toolbar, which gives supporters a chance to raise money for the cause every time they search the Internet or shop online.

 

Once a supporter has added The Leukemia & Lymphoma Society Toolbar to a web browser (like Internet Explorer, Safari or Firefox), each time s/he shops at one of more than 1,300 participating top stores (including Amazon, Target, Apple, Macy’s, Best Buy, Orbitz, Staples and others), LLS will earn a percentage of the purchase price – at no extra cost to the user!

 

The toolbar also includes a Yahoo! powered search box and every time a user searches the web, about a penny is donated to The Leukemia & Lymphoma Society.  The pennies add up - just 5,000 supporters searching four times a day will earn around $73,000 in a year!

 

The Leukemia & Lymphoma Society Toolbar gives supporters at all income levels a tool to help raise funds for our cause.  While doing a search or shopping online, why not raise money for The Leukemia & Lymphoma Society?

 

“We know there are a lot of people who want to do good, but may not have the time or the money to help out.” said Ken Ramberg, Co-Founder of GoodSearch and former President of MonsterTRAK, the largest online career site for college students (now a division of Monster.com). “The new Leukemia & Lymphoma Toolbar makes it as easy as possible.  We’ve taken something people do every day -- searching the Internet and shopping online -- and have turned it into doing good."

0 Comments Permalink

Pioneer in Late Effects Cancer Research Raises Awareness for the  Importance of  Funding  Science for Treatment

 

October 22, 2009

 

See the 'Create a better life for patients'  Op  Ed featured in today's Philadelphia Inquirer.    Dr. Meadows, a long-time supporter of LLS, and renowned oncologist,  is spearheading a campaign to help eliminate the causes of cancer treatment's late effects.

 

To help fund  these  efforts, donate online at www.lls.org/donate.

0 Comments Permalink
1 2 3 4 Previous Next